Other specified coagulation defects

Preferred Label : Other specified coagulation defects;

ICD-10 exclusion note : hemorrhagic disease of newborn (P53);

Diag associé à un acte (%) : 64.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

D688;

UMLS CUI

C0477316;

DO Cross reference
- alpha-2-plasmin inhibitor deficiency [DO Concept]
Orphanet concepts
- Combined deficiency of factor V and factor VIII [ORDO Disease]
- Congenital alpha2-antiplasmin deficiency [ORDO Disease]
- Congenital high-molecular-weight kininogen deficiency [ORDO Disease]
- Congenital plasminogen activator inhibitor type 1 deficiency [ORDO Disease]
- Congenital prekallikrein deficiency [ORDO Disease]
- Familial thrombocytosis [ORDO Disease]
- Familial thrombomodulin anomalies [ORDO Disease]
- Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation [ORDO Disease]
- Protein S acquired deficiency [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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